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dc.creatorHilberg O., Hoffmann-Vold A.-M., Smith V., Bouros D., Kilpeläinen M., Guiot J., Morais A., Clemente S., Daniil Z., Papakosta D., Fretheim H., Neves S., Alfaro T.M., Antoniou K.M., Valveny N., Asijee G., Soulard S., Wuyts W.en
dc.date.accessioned2023-01-31T08:28:11Z
dc.date.available2023-01-31T08:28:11Z
dc.date.issued2022
dc.identifier10.1183/23120541.00597-2021
dc.identifier.issn23120541
dc.identifier.urihttp://hdl.handle.net/11615/73968
dc.description.abstractThe PERSEIDS study aimed to estimate incidence/prevalence of interstitial lung diseases (ILDs), fibrosing interstitial lung diseases (F-ILDs), idiopathic pulmonary fibrosis (IPF), systemic sclerosis-associated ILD (SSc-ILD), other non-IPF F-ILDs and their progressive-fibrosing (PF) forms in six European countries, as current data are scarce. This retrospective, two-phase study used aggregate data (2014–2018). In Phase 1, incident/prevalent cases of ILDs above were identified from clinical databases through an algorithm based on codes/ keywords, and incidence/prevalence was estimated. For non-IPF F-ILDs, the relative percentage of subtypes was also determined. In Phase 2, a subset of non-IPF F-ILD cases was manually reviewed to determine the percentage of PF behaviour and usual interstitial pneumonia-like (UIP-like) pattern. A weighted mean percentage of progression was calculated for each country and used to extrapolate incidence/prevalence of progressive-fibrosing ILDs (PF-ILDs). In 2018, incidence/105 person-years ranged between 9.4 and 83.6 (ILDs), 7.7 and 76.2 (F-ILDs), 0.4 and 10.3 (IPF), 6.6 and 71.7 (non-IPF F-ILDs), and 0.3 and 1.5 (SSc-ILD); and prevalence/105 persons ranged between 33.6 and 247.4 (ILDs), 26.7 and 236.8 (F-ILDs), 2.8 and 31.0 (IPF), 22.3 and 205.8 (non-IPF F-ILDs), and 1.4 and 10.1 (SSc-ILD). Among non-IPF F-ILDs, sarcoidosis was the most frequent subtype. PF behaviour and UIP-like pattern were present in a third of non-IPF F-ILD cases each and hypersensitivity pneumonitis showed the highest percentage of progressive behaviour. Incidence of PF-ILDs ranged between 2.1 and 14.5/105 person-years, and prevalence between 6.9 and 78.0/105 persons. To our knowledge, PERSEIDS is the first study assessing incidence, prevalence and rate of progression of ILDs across several European countries. Still below the threshold for orphan diseases, the estimates obtained were higher and more variable than reported in previous studies, but differences in study design/ population must be considered. © The authors 2022.en
dc.language.isoenen
dc.sourceERJ Open Researchen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85127689408&doi=10.1183%2f23120541.00597-2021&partnerID=40&md5=31935d402e69ae613a21a19120b3888f
dc.subjectalgorithmen
dc.subjectallergic pneumonitisen
dc.subjectArticleen
dc.subjectconnective tissue diseaseen
dc.subjectcontrolled studyen
dc.subjectdiagnostic test accuracy studyen
dc.subjectdisease exacerbationen
dc.subjectfibrosisen
dc.subjectforced vital capacityen
dc.subjecthospitalizationen
dc.subjecthumanen
dc.subjectICD-10en
dc.subjectICD-9en
dc.subjectincidenceen
dc.subjectinterstitial lung diseaseen
dc.subjectinterstitial pneumoniaen
dc.subjectpredictive valueen
dc.subjectprevalenceen
dc.subjectretrospective studyen
dc.subjectrheumatoid arthritisen
dc.subjectsarcoidosisen
dc.subjectsensitivity analysisen
dc.subjectEuropean Respiratory Societyen
dc.titleEpidemiology of interstitial lung diseases and their progressive-fibrosing behaviour in six European countriesen
dc.typejournalArticleen


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